CSA SME
- United States
- Contract
- CAPEX Projects
This is a fantastic opportunity for a CSA SME to join our major, global pharmaceutical client on their latest new-build project based in Indiana, this is a large-scale greenfield capital project and investing more than $1bn.
Reporting to the Design Manager, responsibilities will be:
- To be subject matter expert (SME) on CSA on behalf of client.
- Coordination with the wider multi-disciplinary team for the Delivery of the project
- Act as the Primary interface with CSA engineering providers during the Engineering and construction phase of the project.
- Active participation in design reviews including 3D model reviews
- Define client expectations to Architectural & Engineering designers and ensure delivery in line with this expectation, including the application of standards and guidelines.
- Manage and ordinate interfaces between CSA design and construction with other disciplines included electrical, utilities, HVAC, Process and Mechanical.
- Engage with Third Parties e.g. Contractors, Utility Providers, Insurers, Authorities and other Pfizer groups to ensure compliance and contribute to a successful project delivery.
- Co-ordinate the engagement of internal and external client team members during the CSA design and construction phases
- Ensure overall quality of the CSA design by performing regular reviews.
- Ensure that EHS considerations are appropriately addressed throughout the Engineering phase of the project, including but not limited to HAZOP, constructability reviews and risk review studies.
- Monitor and control Costs and changes to ensure that the project budgets are maintained
Education/Experience
To be successful in this role you will require:
- Applicable higher education degree/diploma
- Five or more years similar work experience exhibiting career progression
- Computer literate with proficiency in Microsoft applications, AutoCAD etc.
- Familiar with Navis Works and BIM 360 a significant advantage
- Previous assignments on Pharmaceutical/Biotechnology Projects would be preferred
- Familiar with clean room design and construction an advantage
- Familiar with GMP manufacturing/Operations an advantage
- Ability to use and interpret technical documents, specifications, drawings, vendor data
- Experience in Projects from commencement to completion
If this role is of interest to you, please apply now!
#LI-AN1
I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
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